mitochondrial myopathies

Preferred Label : mitochondrial myopathies;

CISMeF synonym : Myopathy, Mitochondrial;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0026160;

UMLS CUI

C0162670;

Currated CISMeF NLP mapping
- Mitochondrial Myopathy [NCIt concept]
- Mitochondrial cytopathy (disorder) [SNOMED CT concept]
- Mitochondrial myopathies [ICD-11 Category]
- Mitochondrial myopathy [PASCAL descriptor]
- Mitochondrial myopathy [HPO term]
- Mitochondrial myopathy [MedDRA Preferred Term]
- Mitochondrial myopathy [ORDO Disease]
- Mitochondrial myopathy (disorder) [SNOMED CT concept]
- mitochondrial myopathy [DO Concept]
- mitochondrial myopathy [Disease (Nov.)]
- mitochondrial myopathy [SNOMED Notion]
MeSH narrower concept(s)
- luft disease [MeSH concept]
- megaconial myopathies [MeSH concept]
- pleoconial myopathies [MeSH concept]
Related record
- mitochondrial myopathies [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Mitochondrial Myopathy [NCIt concept]
- Mitochondrial myopathy [ORDO Disease]
- Mitochondrial myopathy [HPO term]
- Mitochondrial myopathy [MedDRA Preferred Term]
- Mitochondrial myopathy (disorder) [SNOMED CT concept]
- Mitochondrial myopathy, episodic, with or without optic atrophy and reversible leukoencephalopathy [OMIM Phenotype]
- Mitochondrial myopathy, not elsewhere classified [ICD-10 Sub-category (who)]
- mitochondrial myopathy [SNOMED Notion]
- mitochondrial myopathy [DO Concept]
- mitochondrial myopathy [Disease (Nov.)]
Validated automatic mappings to BTNT
- Mitochondrial myopathy, episodic, with or without optic atrophy and reversible leukoencephalopathy [OMIM Phenotype]
Validated automatic mappings to NTBT
- disorder of mitochondrial functions [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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